Literature DB >> 75710

A possible mutation of a fluorescence polymorphism.

J A Robinson, K E Buckton, H J Evans.   

Abstract

The segregation of the Q-band polymorphisms in 32 families have been studied. From 90 matings in these families, there were a total of 208 offspring. In one of these offspring it could be shown that there had been a change of a fluorescent polymorphism, resulting in the loss of fluorescent intensity in the satellite of a chromosome 21. The origin of such a 'mutation' and a consideration of mutation rates is discussed.

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Year:  1978        PMID: 75710     DOI: 10.1111/j.1469-1809.1978.tb01899.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  4 in total

Review 1.  Satellite DNA and heterochromatin variants: the case for unequal mitotic crossing over.

Authors:  D M Kurnit
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

2.  Maternal age and origin of non-disjunction in trisomy 21.

Authors:  J F Mattei; S Ayme; M G Mattei; F Giraud
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318

3.  Cytogenetic study of a large black kindred: inversions, heteromorphisms, and segregation analysis.

Authors:  T A Fogle; W H McKenzie
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

4.  Polymorphism of human chromosomes 1, 9, 16, Y: variations, segregation and mosaicism.

Authors:  S Simi; F Tursi
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

  4 in total

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